Analyte sensor
The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.
1. A transcutaneous analyte sensor system comprising:
a transcutaneous glucose sensor having a membrane;
sensor electronics operably connectable to the transcutaneous glucose sensor;
an electrical contact comprising a first material, wherein the first material is associated with a first durometer hardness, wherein the electrical contact is configured to operably connect the transcutaneous glucose sensor to the sensor electronics;
a sealing member comprising a second material, wherein the second material is associated with a second durometer hardness, wherein the sealing member at least partially surrounds the electrical contact and at least a portion of the transcutaneous glucose sensor when the transcutaneous glucose sensor is operably connected to the sensor electronics, wherein the sealing member substantially seals at least a portion of the electrical contact from moisture;
a contact holder over which the sealing member and the transcutaneous glucose sensor are at least partially located; and
wherein the first durometer hardness is higher than the second durometer hardness.
2. The system of claim 1 , wherein the first durometer hardness is from about 5 Shore A to about 80 Shore A.
3. The system of claim 2 , wherein the second durometer hardness is from about 5 Shore A to about 80 Shore A.
4. The system of claim 2 , wherein the second durometer hardness is from about 20 Shore A to about 50 shore A.
5. The system of claim 1 , wherein the contact holder is connected to a mounting unit.
6. The system of claim 1 , wherein the contact holder comprises means for maintaining the sealing member on the contact holder.
7. The system of claim 1 , wherein the contact holder and sealing member comprises means for maintaining the sealing member substantially in place on the contact holder.
8. The system of claim 1 , wherein the sealing member is held at least in part on the contact holder by mating male-female mechanical structures on the contact holder and on the sealing member.
9. The system of claim 1 , wherein the sealing member comprises a raised ridge to improve a seal around the electrical contact.
10. The system of claim 1 , wherein the sealing member is held on the contact holder at least in part by protrusions on the contact holder that are configured to mate with recesses on the sealing member.
11. The system of claim 1 , wherein the sealing member is held on the contact holder at least in part by a chemical to maintain the sealing member substantially stationary without substantial translation or deformation during sensor insertion.
12. A transcutaneous analyte sensor system comprising:
a first component comprising:
a transcutaneous glucose sensor configured for transcutaneous implantation into a body of a host, the transcutaneous glucose sensor comprising:
an electrode; and
a membrane comprising at least one enzyme;
an electrical contact comprising a material associated with a first durometer hardness; and
a sealing member at least partially surrounding a portion of the transcutaneous glucose sensor and at least partially surrounding the elastomeric electrical contact, the elastomeric sealing member comprising a material associated with a second durometer hardness that is less than the first durometer hardness; and
a second component comprising sensor electronics operably connectable to the transcutaneous glucose sensor;
wherein the first component is sterilized with radiation sterilization by exposing the transcutaneous glucose sensor to an electron beam radiation at a dose of about 25 kGy.
13. The system of claim 12 , wherein the membrane is a membrane system comprising a plurality of different membrane layers.
14. The system of claim 12 , wherein the membrane is a membrane layer.
15. The system of claim 12 , wherein the membrane has a thickness from 20 microns to 55 microns.
16. The system of claim 15 , wherein the membrane is a membrane system comprising a plurality of different membrane layers.
17. The system of claim 15 , wherein the membrane is a membrane layer.
18. A transcutaneous analyte sensor system comprising:
a first component comprising:
a transcutaneous glucose sensor configured for transcutaneous implantation into a body of a host, the transcutaneous glucose sensor comprising:
an electrode; and
a membrane comprising at least one enzyme;
an electrical contact comprising a material associated with a first durometer hardness; and
a sealing member at least partially surrounding a portion of the transcutaneous glucose sensor and at least partially surrounding the elastomeric electrical contact, the elastomeric sealing member comprising a material associated with a second durometer hardness that is less than the first durometer hardness; and
a second component comprising sensor electronics operably connectable to the transcutaneous glucose sensor, wherein the sensor electronics are not radiation sterilized, wherein the second component and the first component are configured to be physically coupled during sensor use;
wherein the first component is sterilized with radiation sterilization by exposure to an electron beam radiation;
wherein exposure to the electron beam radiation increases the set of the sealing member or the electrical contact.
19. The system of claim 18 , wherein the dose is about 25 kGy.
20. The system of claim 18 , wherein the membrane is a membrane system comprising a plurality of different membrane layers.
21. The system of claim 18 , wherein the membrane is a membrane layer.
22. The system of claim 18 , wherein the membrane has a thickness from 20 microns to 55 microns.
23. The system of claim 22 , wherein the dose is about 25 kGy.
24. The system of claim 22 , wherein the membrane is a membrane system comprising a plurality of different membrane layers.
25. The system of claim 22 , wherein the membrane is a membrane layer.
26. The system of claim 22 , further comprising a processor, wherein the processor is configured to use information associated with sensor sensitivity to calibrate sensor data derived from the transcutaneous analyte sensor after implantation of an in vivo portion of the transcutaneous analyte sensor into the body of the host, without use of a reference analyte concentration value obtained after implantation of the in vivo portion of the transcutaneous analyte sensor into the body of the host.